Abstract
Antigenic polymorphism of the class I-like maternally transmitted antigen (Mta) is controlled by a maternally transmitted factor (Mtf) thought to reside in mitochondria. However, the mechanisms by which Mtf generates antigenic polymorphism are not known. To address this issue, we investigated a possible role of post-translational oligosaccharide addition in the formation of Mta determinants. We examined the expression of Mta on cytotoxic T lymphocyte (CTL) target cells cultured in tunicamycin (TM), a known inhibitor of asparagine(N)-linked glycosylation. Of 18 Mtab-specific CTL lines, 8 lysed TM-treated Mtaa targets. Furthermore, a subclone of one of these eight lines, 17D5.G2, lysed TM-treated targets from all Mtaa strains tested, regardless of H-2K/D haplotype. On the other hand, this CTL clone did not lyse TM-treated target cells from the Mta null, but H-2 expressing strain B10. CAS2. Therefore expression of this Mtab-like determinant is concordant with the expression of Mtaa and seems unlikely to represent a cross-reactive H-2K/D epitope. Our data suggest that an Mtab-like determinant is expressed on unglycosylated Mtaa molecules. Thus, N-linked oligosaccharides probably prevent the expression of an Mtab-like determinant on the Mtaa molecule. We discuss how Mtf may contribute to Mta polymorphism through glycosylation.
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Abbreviations
- CAB:
-
Con A blast
- CML:
-
cell-mediated lympholysis
- Con A:
-
concanavalin A
- CTL:
-
cytotoxic T lymphocyte
- DMEM:
-
Dulbecco's modified minimum essential medium
- FCS:
-
fetal calf serum
- IL-2:
-
interleukin-2
- LPS:
-
lipopolysaccharide
- mAb:
-
monoclonal antibody
- MLC:
-
mixed leukocyte culture
- mMDM:
-
modified Mishell-Dutton medium
- Mta:
-
maternally transmitted antigen
- NK:
-
natural killer
- sMDM:
-
supplemented Mishell-Dutton medium
- TM:
-
tunicamycin
- β 2m:
-
beta-2 microglobulin
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Han, A.C., Rodgers, J.R. & Rich, R.R. Unglycosylated Mtaa expresses an Mtab-like determinant. Immunogenetics 25, 234–240 (1987). https://doi.org/10.1007/BF00404693
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DOI: https://doi.org/10.1007/BF00404693